**13011BR**
**Title:**

Associate Principal, Regulatory Affairs

**Job Description:**

Responsible for establishing and preparing strategy for worldwide product approval submission activities focused on US/EU/Canada and ensuring compliance to FDA and international regulatory agency requirements for Neurovascular and Peripheral devices. Job duties:

+ Represent Regulatory on project teams and partner with the cross functions on the team to ensure alignment of global regulatory strategy with the team objectives.
+ Identify regulatory requirements for the markets identified in the regulatory strategy.
+ Develop and execute the regulatory strategy for the assigned market(s).
+ Write, review, and file regulatory submissions to ensure MicroVention devices are commercially available in the assigned market(s) based on the approved regulatory strategy.
+ Communicate with regulatory agencies on administrative and routine matters.
+ Document, cons...